Canonical Allele Identifier: PA916018618
Gene: OTOG HGNC NCBI

Linked Data

ClinVar Variation Id: 505067
ClinVar RCV Id: RCV000611036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278992.1:p.Ala5Val
CA218483364
NM_001292063.2:c.14C>T